Neonatal Iron Deficiency Causes Abnormal Phosphate Metabolism by Elevating FGF23 in Normal and ADHR Mice

Iron Deficiency Anemia: A Common and Curable Disease

(2013) J. L. Miller   Cold Spring Harbor Perspectives in Medicine

17β-Estradiol Attenuates Hypoxic Pulmonary Hypertension via Estrogen Receptor–mediated Effects

(2012) Tim Lahm et al.   AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE

Iron status and fibroblast growth factor-23 in Gambian children

(2012) Vickie Braithwaite et al.   BONE

A patient with hypophosphatemic rickets and ossification of posterior longitudinal ligament caused by a novel homozygous mutation in ENPP1 gene

(2011) Tasuku Saito et al.   BONE

Follow-up study of Gambian children with rickets-like bone deformities and elevated plasma FGF23: Possible aetiological factors

(2011) Vickie Braithwaite et al.   BONE

Severe nutritional iron-deficiency anaemia has a negative effect on some bone turnover biomarkers in rats

(2011) Javier Díaz-Castro et al.   EUROPEAN JOURNAL OF NUTRITION

Iron deficiency drives an autosomal dominant hypophosphatemic rickets (ADHR) phenotype in fibroblast growth factor-23 (Fgf23) knock-in mice

(2011) E. G. Farrow et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Loss-of-Function ENPP1 Mutations Cause Both Generalized Arterial Calcification of Infancy and Autosomal-Recessive Hypophosphatemic Rickets

(2010) Bettina Lorenz-Depiereux et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Treatment options for thalassemia patients with osteoporosis

(2010) Evangelos Terpos et al.   Annals of the New York Academy of Sciences

Diagnosis and treatment of iron-deficiency anaemia during pregnancy and postpartum

(2010) Christian Breymann et al.   ARCHIVES OF GYNECOLOGY AND OBSTETRICS

Bone disease and skeletal complications in patients with β thalassemia major

(2010) Rachid Haidar et al.   BONE

Regulation of iron pathways in response to hypoxia

(2010) Nikolai L. Chepelev et al.   FREE RADICAL BIOLOGY AND MEDICINE

An autosomal dominant hypophosphatemic rickets phenotype in a Tunisian family caused by a new FGF23 missense mutation

(2009) Moez Gribaa et al.   JOURNAL OF BONE AND MINERAL METABOLISM